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Acrofrontofacionasal dysostosis

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This is an old revision of this page, as edited by Cydebot (talk | contribs) at 16:38, 20 September 2016 (Robot - Moving category Genetic disorders to Category:Genetic diseases and disorders per CFD at Wikipedia:Categories for discussion/Log/2016 September 12.). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Acrofrontofacionasal dysostosis is an extremely rare disorder, characterized by intellectual disability, short stature, hypertelorism, broad notched nasal tip, cleft lip/palate, postaxial camptobrachypolysyndactyly, fibular hypoplasia, and anomalies of foot structure.

References

  • Richieri-Costa A, Colletto GM, Gollop TR, Masiero D (April 1985). "A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: acro-fronto-facio-nasal dysostosis syndrome". Am. J. Med. Genet. 20 (4): 631–8. doi:10.1002/ajmg.1320200409. PMID 2986457.